[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

CN1174060C - Acrylic modified waterborne alkyd dispersions - Google Patents

Acrylic modified waterborne alkyd dispersions Download PDF

Info

Publication number
CN1174060C
CN1174060C CNB988097559A CN98809755A CN1174060C CN 1174060 C CN1174060 C CN 1174060C CN B988097559 A CNB988097559 A CN B988097559A CN 98809755 A CN98809755 A CN 98809755A CN 1174060 C CN1174060 C CN 1174060C
Authority
CN
China
Prior art keywords
acid
group
water
methacrylate
ester
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
CNB988097559A
Other languages
Chinese (zh)
Other versions
CN1272865A (en
Inventor
M・D・克拉克
M·D·克拉克
赫尔默
B·J·赫尔默
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hexion GmbH
Hexion Inc
Original Assignee
Eastman Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eastman Chemical Co filed Critical Eastman Chemical Co
Publication of CN1272865A publication Critical patent/CN1272865A/en
Application granted granted Critical
Publication of CN1174060C publication Critical patent/CN1174060C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F273/00—Macromolecular compounds obtained by polymerising monomers on to polymers of sulfur-containing monomers as defined in group C08F28/00
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/02—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polycarbonates or saturated polyesters
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F291/00—Macromolecular compounds obtained by polymerising monomers on to macromolecular compounds according to more than one of the groups C08F251/00 - C08F289/00
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/46—Polyesters chemically modified by esterification
    • C08G63/48—Polyesters chemically modified by esterification by unsaturated higher fatty oils or their acids; by resin acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
    • C08G63/688—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
    • C08G63/6884—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur derived from polycarboxylic acids and polyhydroxy compounds
    • C08G63/6888—Polycarboxylic acids and polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/003—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/08—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
    • C09D151/003—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
    • C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Chemical & Material Sciences (AREA)
  • Paints Or Removers (AREA)
  • Polymerisation Methods In General (AREA)
  • Graft Or Block Polymers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

A water-based latex of an acrylic-modified waterborne alkyd dispersion in water is described. The acrylic-modified waterborne alkyd is a hybrid resin prepared by the polymerization of at least one ethylenically unsaturated monomer in the presence of a waterborne alkyd having at least one pendant sulfonate functionality. Preparation of hybrid latexes which contain latent oxidative functional (LOF) acrylic monomers may also be achieved by emulsion polymerization of at least one LOF acrylic monomer in the presence of a waterborne alkyd having at least one pendant sulfonate functionality whereby the latent oxidative functionality of the acrylic polymer survives polymerization. Such acrylic-modified waterborne alkyds are useful in a variety of coating compositions.

Description

Acrylic modified waterborne alkyd dispersions
Background of invention
Invention field
The present invention relates to the water-based latex of a kind of acrylic modified waterborne alkyd dispersions in water.Such acrylic modified waterborne alkyd can be used in the diversified coating composition.
Description of Related Art
In recent years, coatings industry has been made a lot of effort and has been developed low or zero VOC content formulation for coating material.The rules of the VOC content of restriction industrial coating help research and development, to explore the related new technology of solvent discharge of industrial solvent base coating operations such as reducing automobile, electrical equipment, common metal, furniture.A kind of technology relates to uses water to replace organic solvent, and useful especially owing to obvious reason such as availability, cost and environmental acceptability.Yet though brought the health and safety benefit from the organic solvent based composition and use thereof in packaging to the transformation of aqueous composition, water base paint compositions must meet or exceed from the standard of performance of solvent-based compositions expection.Meet or exceed the needs of this type of standard of performance, show the feature and the performance of the waterborne polymeric dispersion liquid that will pay attention to being used for water base paint compositions.
The waterborne polymeric dispersion liquid is each preparation from following three kinds of primary industry film-forming polymer types always: polyester, acrylic acid or the like, and alcohol acids.In these three kinds of polymer types, aqueous alkide resin demonstrates than waterborne polyester or significantly high package stability and the coating stability of acrylic resin.In addition, because its lower molecular weight, Synolac also demonstrates film forming ability especially, thereby makes final coated film that very high gloss be arranged.As with traditional solvent base alkyd, resistance properties is to represent by the autoxidation of this alcohol sorrel is crosslinked.Yet though alkyd has demonstrated and continued to demonstrate hope, their " drying " and/or set time are quite slow, and be all the more so especially at normal temperatures.In the trial at this type of concern, water alcohol acid has been subjected to a lot of attention with the mixture of relative high-molecular-weight propylene acid polymer.
United States Patent (USP) 4,413,073 has described a kind of a kind of pre-generation polymkeric substance and at least a aqueous-based dispersions preparation method who generates the particulate (" heteropolymer particulate ") of the film-forming polymer of polymkeric substance on the spot of comprising.This dispersion liquid is to prepare in the presence of at least 8 amphipathic stable compound at its HLB, and its oleophilic moiety to comprise at least one ethylene linkage unsaturated.This aqueous dispersions can be used as a kind of film forming component of coating composition.
United States Patent (USP) 4,451,596 have described water-dilutable alkyd and the acrylate resin that is used for water-dilutable lacquer system.A kind of preparation method of the water-dilutable resin formulation based on alkyd and acrylic resin has also been described.
But european patent application 0 555 903 has been described a kind of water dispersing and mixing polymkeric substance of unsaturated fatty acids acid functional polyesters.In addition, the aqueous dispersions of a kind of like this mixed polymer that is used for highly filled water base paint compositions and filming with this type of coating composition generation have also been described.
PCT application WO 95/02019 has described a kind of emulsion of water dispersive air-drying resin and the preparation method of this type of emulsion.The mixed emulsion of a kind of Synolac and a kind of acrylic resin has also been described.
The acrylate copolymer or the right and wrong of mixtures are reactive before these, otherwise have the similar group that can in Synolac, exist with aminoplastics reaction such as melamine-formaldehyde resin and the reactive group (as oh group) that only at high temperature reacts.
Brief summary of the invention
One aspect of the present invention is a kind of water-based latex of acrylic modified waterborne alkyd resin.This acrylic modified waterborne alkyd resin is a kind of hybrid resin that obtains from the polymerization in the presence of a kind of water alcohol acid of at least a potential oxidisability official's energy (LOF) Acrylic Acid Monomer, makes resulting hybrid resin have potential oxidisability functionality.It is a kind of by making the method for preparing this type of water-based latex from a kind of hybrid resin polymerization that polymerization obtains in the presence of a kind of water alcohol acid of at least a LOF Acrylic Acid Monomer that the present invention also provides, and makes resulting hybrid resin have potential oxidisability functionality.The present invention further provides the coating composition that contains water-based latex of the present invention.
Detailed description of the invention
The invention provides a kind of water-based latex of acrylic modified waterborne alkyd resin.In a kind of specific embodiments, this latex provides a kind of stable emulsion that Acrylic Acid Monomer a kind of hybrid resin that polymerization obtains in the presence of a kind of water alcohol acid that potential oxidisability official can (LOF) is arranged from least a, the LOF group that makes this Acrylic Acid Monomer keep q.s be used for after film forming or during film forming and other LOF group or pure acid functionality further react.Latex of the present invention is stable when storing under the temperature of room temperature or a little higher than room temperature.Crosslinked when latex of the present invention can influence film forming.Such latex film or film thermofixation at normal temperatures or photochemical solidification.
In water-based latex of the present invention, the acrylic modified waterborne alkyd resin generally exists with the particulate form that is scattered in the water.These particulates generally are spheric.These particulates can be structural or unstructuredness.Structural particulate includes but not limited to core/shell particulate and gradient particulate.Core/shell polymeric particulate also can be prepared into multi-petal shape formula, Pericarppium arachidis hypogaeae form, acorn nut form or immature fruit of Juteleaf Raspberry form.Be more preferably about 20～about 80% (weight) that core segment accounts for described particulate gross weight in such particulate, shell partly accounts for about 80～about 20% (weight) of this particulate gross weight.
The mean particle size range of this mixing latex can be about 25～about 500nm.Size range is about 50～about 300nm preferably, is more preferably about 100～250nm.This epoxy glue lactoconium generally is a spheric.
According to the present invention, the second-order transition temperature of the acrylate moiety of this hybrid resin (Tg) can be up to about 100 ℃.Comparatively in the better embodiment of ideal the present invention, second-order transition temperature better can be preferably in about 0～60 ℃ about below 70 ℃ to latex film forming at normal temperatures.
Acrylic modified waterborne alkyd resin of the present invention, be the polymerization in the presence of a kind of water alcohol acid of (LOF) Acrylic Acid Monomer to prepare, make the potential oxidisability functionality of this Acrylic Acid Monomer can be enough to keep polymerization process by at least a potential oxidisability official.Known any polymerization technique on can use technology.This polymerization can be used as a stage or the multistage charging is carried out.If use the multistage charging, then one or more stages can be contained the LOF Acrylic Acid Monomer.Can use different LOF monomers in different steps.Multipolymer can be used as the acrylate moiety of acid modified alcoholic, and can prepare by making other ethylene linkage unsaturated monomer and the copolymerization of LOF Acrylic Acid Monomer.Better use emulsion polymerization technique, can prepare high-molecular weight polymer with low viscosity because letex polymerization makes.Containing the preparation of emulsion polymer of the acrylic modified waterborne alkyd resin of potential oxidisability functionality, is coating composition crosslinked a kind of possible terms of settlement under for example ambient cure of varied condition of cure, thermofixation and photochemical solidification.
Aqueous alkide resin
A kind of aqueous alkide resin that uses in the water-based latex of the present invention, it can be technical known any aqueous alkide resin, comprise that but any water dissipation, water can disperse or the Synolac of water reducible (can enter in the water), its condition is, but this aqueous alkide resin does not contain the pendant sulfonic acid salt group that can give water fugitiveness, water-dispersible or water vattability.Can be used for aqueous alkide resin of the present invention is, but for example contains those Synolac that other can give the group of water fugitiveness, water-dispersible or water vattability.This class group includes, but not limited to pendant carboxylic acid group and salt and acid anhydride, side chain polyethylene group and other side chain hydrophilic radical, also can make this aqueous alkide resin dissipation, disperse or revert in the water with the technical cosurfactant that oneself knows.The example of this type of Synolac is seen United States Patent (USP) 3,979,346,3,894,798,4,299,742,4,301,048 and 4,497,933, and all these all classify this paper reference as.
In general, aqueous alkide resin can be by making a kind of unary fatty acid, fatty acid ester or naturally occurring partly-hydrolysed oil, a kind of glycol or alcohol how, a kind of polycarboxylic acid and a kind of sulfomonomer or the sulfomonomer adducts that contains at least one sulfomonomer group react and prepare.
Unary fatty acid, fatty acid ester or naturally occurring partly-hydrolysed oil better are selected from formula (I), (II) and (III):
In the formula, the R group is a C 8～C 20Alkyl group.Better the R group is one of following groups:
Figure C9880975500082
The linolic acid residue
Figure C9880975500083
The linolenic acid residue
Figure C9880975500084
The oleic acid residue
Unary fatty acid, fatty acid ester or naturally occurring partly-hydrolysed oil better are by a kind of lipid acid or oil and a kind of many alcohol reactions are prepared.The example that is suitable for oil includes but not limited to Trisun Oil R 80, Tower rape oil, synourin oil, Oleum Cocois, Semen Maydis oil, oleum gossypii seminis, fish oil, Toenol 1140, oiticica oil, soya-bean oil and tung oil, Tallow, beef, Viscotrol C, lard, palm-kernel oil, peanut oil, perilla oil, Thistle oil, (animal) fatty oil, walnut wet goods.Lipid acid includes but not limited to butter (fat) acid, soy(a)-bean oil fatty acid, tetradecanoic acid, Semen Lini acid, Ba Dousuan, a kind of alkanecarboxylic acid that side chain arranged, coconut oil, tall oil fatty acid, sylvic acid, neodecanoic acid, PIVALIC ACID CRUDE (25), Unimac 5680,12-oxystearic acid, cotton seed acid etc. separately or as the suitable examples of oil composition part.
Glycol or many alcohol better are selected from aliphatic diol, alicyclic diol and arylalkyl glycol.The suitable examples of glycol includes but not limited to ethylene glycol, propylene glycol, glycol ether, triglycol, Tetraglycol 99, five glycol, hexaethylene glycol, seven glycol, eight glycol, nine glycol, ten glycol, 1, ammediol, 2,4-dimethyl-2-ethyl own-1, the 3-glycol, 2,2-dimethyl-1, the 2-propylene glycol, 2-ethyl-2-butyl-1, ammediol, 2-ethyl-2-isobutyl--1, ammediol, 1, the 3-butyleneglycol, 1, the 4-butyleneglycol, 1, the 5-pentanediol, 1, the 6-hexylene glycol, 2,2,4-trimethylammonium-1, the 6-hexylene glycol, the sulphur di-alcohol, 1, the 2-cyclohexanedimethanol, 1, the 3-cyclohexanedimethanol, 1, the 4-cyclohexanedimethanol, 2,2,4-trimethylammonium-1,3-pentanediol, 2,2,4-trimethylammonium-1,3-tetramethylene glycol, the p-Xylol glycol, hydroxyl pivalyl hydroxy new pentane acid ester, decamethylene-glycol, the hydrogenation dihydroxyphenyl propane, three (methylol) propane, three (methylol) ethane, tetramethylolmethane, tetrahydroxybutane, threitol, dipentaerythritol, Sorbitol Powder, glycerine, 1,2, the 4-benzenetricarboxylic anhydride, pyromellitic acid dianhydride, two (methylol) propionic acid etc.
Polycarboxylic acid better is selected from a group of following composition: m-phthalic acid, terephthalic acid, phthalic acid (acid anhydride), hexanodioic acid, tetrachlorophthalic tetrachlorophthalic anhydrid, Tetra Hydro Phthalic Anhydride, dodecanedioic acid, sebacic acid, nonane diacid, 1,4-cyclohexane dicarboxylic acid, 1,3-cyclohexane dicarboxylic acid, maleic anhydride, fumaric acid, succsinic acid (acid anhydride), 2,6-naphthalene dicarboxylic acids, pentanedioic acid and ester thereof.
Except that how pure quantity according to better step and lipid acid, fatty acid ester or naturally occurring partly-hydrolysed oil reaction, can also use many alcohol of additional quantity or other branching agent for example polycarboxylic acid increase the molecular weight and the branching of aqueous alkide resin.These branching agents better are selected from three (methylol) ethane, tetramethylolmethane, tetrahydroxybutane, threitol, dipentaerythritol, Sorbitol Powder, glycerine, 1,2,4-benzenetricarboxylic anhydride, pyromellitic acid dianhydride, two (methylol) propionic acid and three (methylol) propane.
In order to make this Synolac can be used as the reactive coalescents (by the oxidisability coupling) in epoxy glue Ruzhong and to enter in the cross-linked polymer film, be preferably this alkyd have certain limited oily length-length, in or short.This limited oily length or oil-contg are benchmark with the gross weight of this Synolac, are generally about 20% (weight)～about 90% (weight) in this alcohol acid composition.Gross weight with Synolac is a benchmark, and the oily length of " length " oleyl alcohol acid or oil-contg are about 60～90% (weight).Gross weight with Synolac is a benchmark, " in " oil-contg of oleyl alcohol acid is about 40～60% (weight).Gross weight with Synolac is a benchmark, and the oily length of " weak point " oleyl alcohol acid or oil-contg are about 20～40% (weight).
Potential oxidisability official can (LOF) Acrylic Acid Monomer
Will carry out polymerization in the presence of water alcohol acid can (LOF) Acrylic Acid Monomer can be that any to contain Acrylic Acid Monomer LOF group that at least 1 potential oxidisability official can (LOF) group can be that any energy (i) is kept this polymerization process and (ii) participated in or the fragment side chain of the oxidative crosslinking of promotion acid modified alcoholic with the potential oxidisability official that generates water-based latex of the present invention.Behind the LOF polymerizable acrylic monomer, acid modified alcoholic of the present invention has enough LOF groups increases or amplifies the degree of crosslinking of surveying usually in the Synolac.In other words, still have enough LOF groups to increase the effectively crosslinked of this Synolac.
The existence of LOF group on this acid modified alcoholic, the crosslinked possibility that becomes when making film forming or after the film forming.Acid modified alcoholic of the present invention has been arranged, crosslinked just can be between the LOF of the Acrylic Acid Monomer group, taking place between the unsaturated functionality of the ethylene linkage of the LOF of Acrylic Acid Monomer group and alkyd or between the unsaturated functionality of the ethylene linkage of alkyd.The LOF group of oxidizing reaction can take place, and as a radical source that can produce the free radical flux, participates in or promotes oxidn sexual intercourse connection.Be preferably, this LOF group is that a kind of ethylene linkage is unsaturated, such as but not limited to allyl group and vinyl groups.The LOF group better also can be acetoacetyl segment or enamine segment.In the United States Patent (USP) 5,296,530,5,494,975 and 5,525,662 of classifying this paper reference as, narrated enamine preparation from the acetoacetyl group.
There is the example of the Acrylic Acid Monomer of potential oxidisability official's energy (LOF) group to include but not limited to allyl methacrylate(AMA), methacrylic vinyl acetate, methacrylic acid acetoacetyl 2-ethoxyethyl acetate, methacrylic acid hydroxyl butene esters, toxilic acid allyl ester or diallyl, poly-(allyl glycidyl ether) etc.
The acrylate moiety of this acid modified alcoholic can be a kind of homopolymer, also can be a kind of multipolymer.When in the presence of water alcohol acid, carrying out polymkeric substance, this LOF Acrylic Acid Monomer can add separately, also can be with the form of mixtures of multiple LOF Acrylic Acid Monomer, or add with the form of mixtures of LOF Acrylic Acid Monomer and one or more ethylene linkage unsaturated comonomers.The example of the ethylene linkage unsaturated comonomer that is suitable for includes but not limited to styrene monomer, for example vinylbenzene, alpha-methyl styrene, vinyl naphthalene, Vinyl toluene, 1-chloro-4-methyl-benzene etc.; The unsaturated chemical seed of ethylene linkage, for example methyl acrylate, vinylformic acid, methacrylic acid, methyl methacrylate, ethyl propenoate, Jia Jibingxisuanyizhi, butyl acrylate, butyl methacrylate, isobutyl acrylate, Propenoic acid, 2-methyl, isobutyl ester, EHA, ethylhexyl methacrylate, Octyl acrylate, Octyl methacrylate, glycidyl methacrylate, methacrylic acid carbodiimide ester, Ba Dousuan alkane ester, vinyl-acetic ester, n-butyl maleate, dioctyl maleate etc.; Nitrogen containing monomer, comprise t-butylaminoethyl methacrylate, dimethylaminoethyl methacrylate, diethyl aminoethyl methacrylate, N, N-dimethylaminopropyl Methacrylamide, methacrylic acid 2-tertiary butyl amino ethyl ester, vinylformic acid N, N-dimethylamino ethyl ester, N-(2-methacryloxyethyl) ethylidene-urea and methacryloyl amido ethyl ethylidene-urea.Better be that this LOF Acrylic Acid Monomer adds with the form of mixtures of at least a LOF Acrylic Acid Monomer and a kind of ethylene linkage unsaturated comonomer.Be more preferably, this ethylene linkage unsaturated comonomer is a styrene monomer.
Water-based latex
Water-based latex of the present invention be by make at least a potential oxidisability official can (LOF) Acrylic Acid Monomer in the presence of a kind of a kind of aqueous dispersions of water alcohol acid polymerization prepare.Water-based latex of the present invention is stable when the pH identical with the latex for preparing from traditional water alcohol acid.Yet, with traditional water alcohol acid to mix latex different, o'clock be stable based on the present invention's mixing latex of water alcohol acid in pH≤7.In water-based latex of the present invention, acid modified alcoholic generally exists with particulate form in the water.As discussed above, keep enough LOF groups and can make the film generation oxidative crosslinking that generates from resultant water base alkyd latex.Because the LOF group has effectively crosslinked function of this alkyd of raising, thereby survival makes it that not only the coreactivity that reacts with other LOF group and/or water alcohol acid functionality is arranged when film forming or after the film forming after the polymerization of enough LOF groups, and can promote the similar oxidative crosslinking between the water alcohol acid functionality.A result as this type of coreactivity between LOF group and/or the pure acid functionality can obtain better film properties.
As discussed above, LOF Acrylic Acid Monomer or the mixture that can be used as at least a LOF Acrylic Acid Monomer adds, or can be used as the mixture interpolation of at least a LOF Acrylic Acid Monomer and a kind of ethylene linkage unsaturated comonomer.The interpolation of LOF Acrylic Acid Monomer is carried out with one-stage process or multistage (for example core-shell) method.Better, the LOF Acrylic Acid Monomer adds with one-stage process.Can make a kind of even acrylate copolymer (being simple terpolymer) by add LOF Acrylic Acid Monomer (one or more) with one-stage process, the latter contain when film forming or after the film forming can and other LOF group or pure acid functionality reaction or can promote q.s LOF group (for example allyl group, the vinyl) number of the reaction between each functionality on this alkyd.The LOF Acrylic Acid Monomer adds with multiple process can produce a kind of inhomogeneous acrylate copolymer.For example, in two-stage method, first section interpolation may produce a kind of core polymkeric substance, better is a kind of often with the polyfunctional monomer for example vinylformic acid or the styrene/acrylic polymkeric substance of three vinylformic acid three (methylol) propane ester precrosslink.Second section is added a kind of shell polymeric of generation, better is a kind of styrene/acrylic polymkeric substance that contains for example reactive allyl group of high-level LOF group and/or vinyl segment.The monomer that uses in one or more snippets polymerization technique has description in the United States Patent (USP) 5,539,073 of classifying this paper reference as more like this.The LOF group can be positioned at polymer ends, also can distribute along polymer backbone.
As discussed above, better, water-based latex of the present invention prepares under the letex polymerization condition.In general, during the letex polymerization of this LOF acrylic polymer compositions, it mainly is unsaturated segment of acrylic acid ethylene linkage rather than LOF group that polymeric takes place.If the LOF group participates in polymerization, then polymerizing condition should make enough LOF groups survive, in the hope of when the film forming or after the film forming with other LOF group and/or water alcohol acid functionality generation oxidative crosslinking, and/or strengthen oxidative crosslinking between the water alcohol acid functionality.The survival of LOF group such as allyl group or vinyl segment can realize by the reactive difference of handling the ethylene linkage unsaturated group during polymerization.For example, the unsaturated vinylformic acid segment of the ethylene linkage of the Acrylic Acid Monomer of allyl group or vinyl-functional, the reactivity during with the styrene monomer polymerization is greater than LOF allyl group or vinyl segment.As a result, the polymers obtained LOF group that contains.The description of the pulsating survival of allyl group can be consulted the United States Patent (USP) 5,539,073 of classifying this paper reference as when handling the allyl functional acrylic polymer compositions with the promotion letex polymerization.The vinyl-functional acrylic polymer compositions can be to handle with being applicable to the similar mode of allyl functional acrylic polymer compositions.
When the LOF of acrylate copolymer group was an acetoacetyl oxygen segment, polymeric was the unsaturated segment of ethylene linkage under the letex polymerization condition.This acetoacetyl oxygen segment is not influenced by polymerization process, thereby can survive.
The polymerization process that is used for preparing this mixing latex also may need initiator, reductive agent or catalyzer.The initiator that is suitable for comprises initiator commonly used, for example ammonium persulphate, volatile salt, hydrogen peroxide, t-butyl hydroperoxide, ammonium or alkali metal sulfates, dibenzoyl peroxide, lauroyl peroxide, di-t-butyl peroxide, 2,2 '-Diisopropyl azodicarboxylate, benzoyl peroxide etc.
The reductive agent that is suitable for is those persons that can improve the polymerization velocity, and for example comprise sodium bisulfite (sodium bisulfite), sodium bisulfite (sodium hydrosulfite), sodium sulfoxylate formaldehyde, xitix, saccharosonic acid, and composition thereof.
Thereby being those, the catalyzer that is suitable under polymeric reaction condition, can promote polymerization starter to decompose the compound that improves polymerization velocity.The catalyzer that is suitable for comprises transistion metal compound and siccative.The example of this type of catalyzer include but not limited to the inferior cobalt of ferrous sulfate heptahydrate, iron protochloride, copper sulfate, cupric chloride, cobaltous acetate, sulfuric acid, and composition thereof.
Randomly, in the suspension or emulsion polymerization prepared of the present invention's mixing latex, also can use conventional surfactant or combinations-of surfactants as co-stabilizer or cosurfactant, for example anionic or nonionic emulsifier.The example of tensio-active agent includes but not limited to any combination of alkyl-sulphate, alkylsulphonic acid or lipid acid, ethoxylated alkyl phenols or anionic or the nonionic surface active agent of basic metal or ammonium preferably.Better surfactant monomer is HITENOL HS-20 (is polyoxyethylene alkyl phenyl ether ammonium sulfate, can available from the DKS international corporation of Japan).A appropriate table surface-active agent inventory is arranged: the Emulsifier ﹠amp of McCutcheon in the following monograph; Detergents, North America version and international version, MC publishing company, Glenn Roc city, New Jersey, 1993.When the pure acid moieties of Synolac accounts for reaching 35% (weight), when being generally about 5～20% (weight), better using a kind of conventional surfactant or combinations-of surfactants of this latex total solids.
If the mixing latex that obtains is the typical case uses in alkydpaints siccative salt prepare and also the LOF segment be present in the acrylate moiety of alkyd, then except that other performance, also observe the remarkable improvement of latex gelling part and swelling ratio (being respectively LGF and LSR).Though the pure acid moieties that mixes latex is at stabilized latex and improve film forming this all plays a significant role aspect two, what allow better physics and film properties machinery is the existence of LOF acrylate moiety in this alkyd.The performance of improving is that to contain the observed taller cross-linking density of hybrid resin of non-LOF acrylate moiety relevant with comparison.
In general, the pure acid moieties of this mixing latex accounts for about 5～60% (weight) of this latex total solids, better about 10～50% (weight), better about 20～40% (weight), and the acrylate moiety of this mixing latex accounts for about 30～90% (weight) of this latex total solids, better about 50～80% (weight), better about 60～80% (weight).This type of mixes latex can be further used for coating composition.
Coating composition of the present invention contains the latex of acrylic modified waterborne alkyd dispersions of the present invention, and can prepare with technical known technology, for example United States Patent (USP) the 4th, the 698,391, the 4th, 737, No. 551 and the 3rd, those that disclose in 345, No. 313, this paper reference all classified in full as in each piece of writing of these patents.The example of this type of coating composition comprises, for example, and building coating, maintenance finish, industrial coating, car paint, weaving coating, printing ink, tackiness agent and paper, wood and paint for plastics.Coating composition of the present invention contains significantly less solvent, is less than 25% (weight) to low 1% (weight) and even the zero VOC content of reaching.The water alcohol acid of this hybrid resin partly keeps the ideal performance of alkyd, and the LOF acrylate moiety of this resin replenishes or strengthened the crosslinked ability of normal temperature oxidation of this alcohol mixture acid resin.Coating composition of the present invention can produce have high gloss, piece solidifies and the coating of good acid-fast alkali-proof.
This coating composition can be applied on the base material and curing (for example, spray the wet coating of 3～4 mils on metal sheet, and heated 30 minutes in 150 ℃ of forced air stoves) with technical known technology.This base material can be any acceptable substrate, for example paper, polyester film for example polyethylene and polypropylene, metal for example aluminium and steel, glass, polyurethane elastomer, priming paint (japanning) base material etc. is arranged.Coating composition of the present invention can be in self-vulcanizing (ambient cure), at hot setting (thermofixation) or photochemical solidification.
Coating composition of the present invention can further contain paint additive.The example of this type of paint additive includes but not limited to one or more flow agents, rheological agent and flow control agent, for example type siloxane, fluorine carbon or cellulose family; Extender; Reactive coalescing aid is for example classified the U.S. Patent No. 5,349 of this paper reference, those described in 026 as; Softening agent; Matting agent; Pigment wetting and dispersion agent and tensio-active agent; Ultraviolet (UV) absorption agent; UV light stabilizing agent; Tinting pigment; Tinting material; Defoamer and antifoams; Anti-settling, antitrickle and thickening material; Anti; Anti-floating and anti-floating agent; Biocide, mycocide and mould inhibitor; Inhibiter; Thickening material; Or coalescing agent.The specific examples of examples of such additives can be consulted Raw Materials Index, and (1500 Rhode Island Avenue, N.W.Washington D.C.20005) publish whole nation paint with coating association.The further example of examples of such additives and emulsion polymerisation process opinion can be consulted the U.S. Patent No. 5,371,148 of classifying this paper reference as.
The example of matting agent includes but not limited to that synthetic silica (can be available from W.R.Grace ﹠amp; The Davison Chemical Division of Company, trade(brand)name SYLOID _); Polypropylene (can be available from Hercules company, trade(brand)name HERCOFLAT _); And synthetic silicate (can be available from J.M.Huber company, trade(brand)name ZEOLEX _).
The example of dispersion agent and tensio-active agent includes but not limited to sulfo-succinic acid two (n-tridecane ester) sodium, sulfo-succinic acid two (2-ethylhexyl) sodium, sulfo-succinic acid dihexyl sodium, sulfo-succinic acid two cyclohexyl sodium, diamyl sodium sulfosuccinate, sulfo-succinic acid diisobutyl ester sodium, sulfo-succinic acid isodecyl ester disodium, sulfo-succinic acid ethoxylated alcohol Carbenoxolone Sodium, sulfo-succinic acid alkylamidoalkyl polyethoxye ester disodium, N-(1,2-dicarboxyl ethyl)-N-(octadecyl) sulfosuccinamic acid four sodium, N-(octadecyl) sulfosuccinamic acid disodium, the sulfated ethoxylated nonylphenol, 2-amino-2-methyl-1-propanol etc.
The example of viscosity, suspension and flow control agent includes but not limited to the high molecular weight carboxylic salt of polyaminoamide phosphate, polyaminoamide and the alkylidene group amine salt of unsaturated fatty acids, all can be available from U.S. BYK Chemie company, commodity are called ANTI TERRA _Further example comprises the Natvosol, hydroxypropylcellulose, polyamide wax, polyolefin-wax, carboxymethyl cellulose, ammonium polyacrylate, sodium polyacrylate, Vltra tears, Type 3U, polyethylene oxide, guar gum of polysiloxane copolymer, polyacrylate solution, cellulose ester, Natvosol, hydrophobically modified etc.Other example of thickening material comprises methylene radical/ethylidene oxide association thickening material and water-soluble carboxyl thickening material, for example UCARPOLYPHOBE of Union Carbide Corporation _
Several patent antifoams are commercial getting, and comprise the BUBREAK such as Buckman laboratory (company) _, the BYK of U.S. BYK Chemie company _, the FOAMASTER of Henkel Corp./coatings chemistry portion _And NOPCO _, the DREWPLUR of the Drew Department of Industry of AShland chemical company _, the TRYSOL of Troy chemical company _And TROYKYD _And the SAG of Union Carbide Corporation _
The example of mycocide, mould inhibitor and biocide includes but not limited to 4, the 4-dimethyl
Figure C9880975500151
Azoles alkane, 3,4, the 4-trimethylammonium
Figure C9880975500152
Azoles alkane, modified barium metaborate, N-methylol-N-methyl dithiocarbamic acid potassium, 2-(thiocyanogen methylthio group) benzothiazole, potassium dimethyldithiocarbamate, diamantane, N-(trichloro-methylthio) phthalic imidine, 2,4,5,6-daconil M, orthoxenol, 2,4,5-Trichlorophenol, dehydroacetic acid (DHA), copper naphthenate, cupric octoate, organoarsenic, tributyltin oxide, zinc naphthenate and 8-quinolinic acid copper.
The example of uv-absorbing agent and UV light stabilizing agent among others, also includes substituted benzophenone, benzotriazole, the hindered amines of replacement and the benzoate that is obstructed is arranged, can be available from the trade(brand)name CYASORB UV of U.S. Cyanamid company _With 3-ethanoyl-4-hydroxybenzyl diethyl phosphonate, 4-(12 carbon alkoxyl group)-2-hydroxyl diphenylketone and Resorcinol one benzoic ether.
The example of solvent and coalescing agent is known, and includes but not limited to ethanol, n-propyl alcohol, Virahol, propyl carbinol, sec-butyl alcohol, isopropylcarbinol, ethylene glycol-ether, propylene glycol n-butyl ether, propylene glycol-methyl ether, propylene glycol-propyl ether, two polypropylene glycols-methyl ether, glycol ether-butyl ether, neopentyl glycol-isobutyrate, ethylene glycol-octyl ether, Pyranton, TEXANOL _Ester alcohol (Eastman chemical company) etc.Such solvent and coalescing aid also can comprise reactive solvents and coalescing aid, for example the SANTOLINK XI-100 of diisopropyl phthalate, Monsanto Company _Poly epihydric alcohol base allyl ethers, and classify other material described in the United States Patent (USP) the 5th, 349, No. 026 and the 5th, 371, No. 148 of this paper reference as.
Be suitable for the pigment in the contemplated coating composition of the present invention, be well-known typical pigment dyestuff of personnel and the mineral dye that the general technical ability of topcoating technology is arranged, particularly ColourIndex (the 3rd edition the 2nd revision, nineteen eighty-two, dyer and colorist association and U.S. textile chemist and colorist association combined publication) in enumerate those.Example includes but not limited to following: titanium dioxide, barite, clay, or lime carbonate, No. 6, CI Pigment white (titanium dioxide); No. 101, CI Pigment red (red iron oxide); No. 42, CI Pigment Yellow 73; CI pigment Blue 15 number, 15: No. 1,15: No. 2,15: No. 3,15: No. 4 (CuPc); CI pigment red 49: No. 1; With CI Pigment red 57: No. 1.Tinting materials such as phthalocyanine blue, molybdate orange or carbon black also are applicable to coating composition of the present invention.
Provide following example the present invention is described.Yet, should be understood that, the invention is not restricted to specified conditions described in these examples or details.
The following material of not describing more than the example of the various coating compositions of the present invention uses:
COBALT HYDROCURE II catalyzer, OMG company sells, joslyn hi-voltage;
The DOWFAX2AI tensio-active agent derives from Dow Chemical Company, the state of Michigan, Midland;
KELSOL 3960-B2G-75,3922-G-80,3964-B2G-70 and 3904-BG4-75 water-dilutable alkyd, Reichhold chemical company sells, research triangle garden, the North Carolina state;
TERGITOL 15-S-40 tensio-active agent, associating carbide chemical and Plastics Company are sold, Connecticut State Danbury;
TEXANOL ester alcohol coalescing agent, Yisiman Chemical Company sells, field sodium Xi Zhou, this baud of gold.
With coating and the film of following method assessment according to the present invention's preparation.
Film gel section/swelling ratio
Films swell is by being determined in the acetone recently obtaining of the dry weight of soluble weight fraction in the soluble polymer weight mark of swollen (by weight) and dry film sample than (FSR).
Used program is as follows: for each sample determination, all have one 4 " * 4 " 325 order steel sieves and metal boat of weighing to be placed on kiln roasting, cool off 30 minutes, weigh (being respectively W1 and W2).The latex film drying, after room temperature keeps required fate, cut one piece of film, weigh (W3), be placed in the aluminium dish, set aside.Cut another piece film sample, weigh (W4), put in the screw-cap wide-necked bottle that excessive solvent arranged, on the constant temperature wobbler is bathed, placed 16 hours.By this solution humidification solid is toppled over via screen cloth and with screen cloth add the contained wet solid that stays weigh (W5) reclaim the film gel.At this moment, allow screen cloth add solid and film sample is placed in the aluminium boat, in 80 ℃ vacuum drying oven, be dried to constant weight, obtain the weight (W7) that screen cloth adds film sample in dried solid weight (W6) and the aluminium boat.Calculating shows below:
FGF＝(W6-W1)/[W4*((W7-W2)/W3)]
FSR＝(W5-W1)/(W6-W1)
The preparation of example 1～8:KELSOL alkyd/acrylic acid mixture
With a series of alkyd/acrylic acid mixtures that can disperse alkyd resin production of the KELSOL shown in the table 1.The type of the LOF content in these mixtures, pure acid content and alkyd all is different.
The general step for preparing these materials is as follows: add an amount of softening water and alkyd in a 500ml reactor, and the ammonium hydroxide of capacity is 8.0 to regulate pH.Inclusion in the reactor is heated to 82 ℃, after this uses 240 fens clock times that 2.06g Dowfax 2AI (disodium 4-dodecyl-2,4 '-oxydibenzenesulfonate of Dow Chemical Company's supply) and the solution of 0.93g ammonium persulphate in 22g water are joined in this reactor.Simultaneously, add the monomer mixture shown in the 176g table 2 with 225 fens clock times.When finishing in these 225 minutes, add the 9g methyl methacrylate with 15 fens clock times.After interpolation finishes, reactor was kept 1 hour at 82 ℃, then cool to room temperature.The mixture that will contain 0.2g tert-butyl peroxide and 2.75g water at last joins in this latex with the mixture that contains 0.2g sodium formaldehyde sulphoxylate and 2.75g water, and mixes.Then this latex is filtered by 100 order wire cloths.The granularity of the mixing latex that is generated, pH and percentage solid content are listed in the table 2.
Table 1 KELSOL can disperse Synolac
KELSOL alkyd The percentage solid content Acid number
3922-G-80 80 52-58
3960-B2G-75 75 37-41
3964-B2G-70 70 38-42
3904-BG4-75 75 38-42
Table 2
Latex KELSOL alcohol acid type Alkyd 1 Monomer mixture ratio MMA/BA/AAEM 2 Granularity (nm) pH Tg ℃ Fragment (g) Solid content (%)
1 3922-G-80 9.1 60/40 60 6.0 27 14.5 47.1
2 3922-G-80 9.1 55/35/10 68 5.4 37 2.3 44.8
3 3922-G-80 9.1 50/30/20 82 5.5 38 5.9 47.0
4 3922-G-80 16.7 55/35/10 48 6.0 31 1.4 44.9
5 3922-G-80 23.1 55/35/10 41 6.2 29 2.9 44.9
6 3960-B2G-75 9.1 55/35/10 92 5.7 - 22.1 44.9
7 3964-B2G-70 9.1 55/35/10 78 5.5 - 4.6 44.9
8 3904-BG4-75 9.1 55/35/10 85 5.7 - 4.8 45.1
1. based on the weight % of polymer solids total amount,
2.MMA-methyl methacrylate, BA-butyl acrylate, AAEM-methacrylic acid ethanoyl acetyl oxygen ethyl ester.
Example 9: the film gel section of example 1-8 and film swelling ratio
For each latex of example 1-8, in 50g latex, add 0.32g 28% ammonium hydroxide, the 2.7g25% TERGITOL 15-S-40 aqueous solution, 1.1gTEXANOL and 0.45gCobalt HYDROCURE II.With this latex solution casting film-forming, one week of dry air at room temperature then.Measure film according to the method described above and coagulate part (FGF) and film swelling ratio (FSR), different is usefulness tetrahydrofuran (THF) (THF) is as solvent, rather than with acetone as solvent.
As non-sense in the same old way example 1 is compared with the system that contains as the AAEM of LOF, had much higher FSR and much lower FGF.The example 3 that LOF content is the highest has minimum FSR and the highest FGF.
The film swelling ratio of table 3 example 1-8 and film gel section
The latex instance number The film swelling ratio The film gel section
1 33.9 0.36
2 8.7 0.80
3 3.9 0.89
4 6.6 0.81
5 6.3 0.82
6 17.1 0.57
7 15.3 0.62
8 9.2 0.76

Claims (18)

1. acrylic acid modified alkyd resin, comprise the polymerisate of at least a potential oxidisability functionalized propylene's acid mono in the presence of a kind of water alcohol acid, its condition is that this water alcohol acid does not contain pendant sulfonic acid salt group, wherein, described acrylic modified alkyd has abundant for the potential oxidisability functional group that utilizes, thereby can increase the effectively crosslinked of described alkyd on being applied to base material the time.
2. the acrylic acid modified alkyd resin of claim 1, wherein, potential oxidisability functional group is selected from one group that is made up of allyl group, vinyl, acetoacetyl and enamine.
3. the acrylic acid modified alkyd resin of claim 1, wherein, described latent oxidatively-functional Acrylic Acid Monomer is selected from one group that is made up of following: allyl methacrylate(AMA), methacrylic vinyl acetate, methacrylic acid acetoacetyl 2-ethoxyethyl acetate, methacrylic acid hydroxyl butene esters, toxilic acid-allyl ester, diallyl maleate and poly-(allyl glycidyl ether).
4. the acrylic acid modified alkyd resin of claim 1, wherein, described potential oxidisability functionalized propylene's acid mono is the mixture of at least a latent oxidatively-functional Acrylic Acid Monomer and at least a ethylene linkage unsaturated comonomer.
5. the acrylic acid modified alkyd resin of claim 4, wherein, described ethylene linkage unsaturated comonomer is selected from by vinylbenzene, alpha-methyl styrene, vinyl naphthalene, Vinyl toluene, 1-chloro-4-methyl-benzene, methyl acrylate, vinylformic acid, methacrylic acid, methyl methacrylate, ethyl propenoate, Jia Jibingxisuanyizhi, butyl acrylate, butyl methacrylate, isobutyl acrylate, Propenoic acid, 2-methyl, isobutyl ester, EHA, ethylhexyl methacrylate, Octyl acrylate, Octyl methacrylate, glycidyl methacrylate, methacrylic acid carbodiimide ester, Ba Dousuan alkane ester, vinyl-acetic ester, n-butyl maleate, dioctyl maleate, t-butylaminoethyl methacrylate, dimethylaminoethyl methacrylate, diethyl aminoethyl methacrylate, N, N-dimethylaminopropyl Methacrylamide, methacrylic acid 2-tertiary butyl amino ethyl ester, vinylformic acid N, the N-dimethylamino ethyl ester, N-(2-methacryloxyethyl) ethylidene-urea, form with methacryloyl amido ethyl ethylidene-urea one group.
6. the acrylic acid modified alkyd resin of claim 5, wherein, described ethylene linkage unsaturated comonomer is selected from one group that is made up of vinylbenzene, alpha-methyl styrene, vinyl naphthalene, Vinyl toluene and 1-chloro-4-methyl-benzene.
7. water-based latex, comprise water and a kind of acrylic acid modified alkyd resin, the latter comprises the polymerisate of at least a potential oxidisability functionalized propylene's acid mono in the presence of a kind of water alcohol acid aqueous dispersions that does not conform to pendant sulfonic acid salt group, wherein, described acrylic modified alkyd has abundant for the potential oxidisability functional group that utilizes, thereby can increase the effectively crosslinked of described alkyd on being applied to base material the time.
8. the water-based latex of claim 7, wherein said acrylic modified alkyd comprise with this latex total solids and are 5～60 weight % aqueous alkide resins of benchmark and are the potential oxidisability functionalized propylene's acid mono of 40～95 weight % of benchmark with this latex total solids.
9. the water-based latex of claim 7 further comprises a kind of cosurfactant, and wherein this aqueous alkide resin accounts for 5～35 weight % of this latex total solids.
10. the water-based latex of claim 7, wherein, potential oxidisability functional group is selected from one group that is made up of allyl group, vinyl, acetoacetyl and enamine.
11. the water-based latex of claim 7, wherein, described latent oxidatively-functional Acrylic Acid Monomer is selected from one group that is made up of following: allyl methacrylate(AMA), methacrylic vinyl acetate, methacrylic acid acetoacetyl 2-ethoxyethyl acetate, methacrylic acid hydroxyl butene esters, toxilic acid-allyl ester, diallyl maleate and poly-(allyl glycidyl ether).
12. the water-based latex of claim 7, wherein, described potential oxidisability functionalized propylene's acid mono is the mixture of at least a latent oxidatively-functional Acrylic Acid Monomer and at least a ethylene linkage unsaturated comonomer.
13. the water-based latex of claim 12, wherein, described ethylene linkage unsaturated comonomer is selected from by vinylbenzene, alpha-methyl styrene, vinyl naphthalene, Vinyl toluene, 1-chloro-4-methyl-benzene, methyl acrylate, vinylformic acid, methacrylic acid, methyl methacrylate, ethyl propenoate, Jia Jibingxisuanyizhi, butyl acrylate, butyl methacrylate, isobutyl acrylate, Propenoic acid, 2-methyl, isobutyl ester, EHA, ethylhexyl methacrylate, Octyl acrylate, Octyl methacrylate, glycidyl methacrylate, methacrylic acid carbodiimide ester, Ba Dousuan alkane ester, vinyl-acetic ester, n-butyl maleate, dioctyl maleate, t-butylaminoethyl methacrylate, dimethylaminoethyl methacrylate, diethyl aminoethyl methacrylate, N, N-dimethylaminopropyl Methacrylamide, methacrylic acid 2-tertiary butyl amino ethyl ester, vinylformic acid N, the N-dimethylamino ethyl ester, one group of forming of N-(2-methacryloxyethyl) ethylidene-urea and methacryloyl amido ethyl ethylidene-urea.
14. a coating composition comprises the water-based latex and at least a one group the additive that is selected from following composition of claim 7: rheological agent and flow control agent; Extender; Reactive coalescing aid; Softening agent; Matting agent; Pigment wetting and dispersion agent and tensio-active agent; Ultraviolet (UV) absorption agent; UV light stabilizing agent; Tinting pigment; Tinting material; Defoamer and antifoams; Anti-settling, antitrickle and thickening material; Anti; Anti-floating and anti-floating agent; Biocide, mycocide and mould inhibitor; Inhibiter; Thickening material, and coalescing agent.
15. method for preparing water-based latex, comprise and make at least a latent oxidatively-functional Acrylic Acid Monomer in the presence of a kind of water alcohol acid aqueous dispersions that does not contain pendant sulfonic acid salt group, step of polymerization under the condition of the potential oxidisability functionality survival that is enough to make Acrylic Acid Monomer.
16. the method for claim 15, wherein, potential oxidisability functional group is selected from one group that is made up of allyl group, vinyl, acetoacetyl and enamine.
17. the method for claim 15, wherein, described latent oxidatively-functional Acrylic Acid Monomer is selected from one group that is made up of following: allyl methacrylate(AMA), methacrylic vinyl acetate, methacrylic acid acetoacetyl 2-ethoxyethyl acetate, methacrylic acid hydroxyl butene esters, toxilic acid-allyl ester, diallyl maleate and poly-(allyl glycidyl ether).
18. the method for claim 15, wherein, this polymerization is a kind of letex polymerization.
CNB988097559A 1997-08-12 1998-08-12 Acrylic modified waterborne alkyd dispersions Expired - Lifetime CN1174060C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US5514097P 1997-08-12 1997-08-12
US60/055,140 1997-08-12

Publications (2)

Publication Number Publication Date
CN1272865A CN1272865A (en) 2000-11-08
CN1174060C true CN1174060C (en) 2004-11-03

Family

ID=21995893

Family Applications (2)

Application Number Title Priority Date Filing Date
CNB988097559A Expired - Lifetime CN1174060C (en) 1997-08-12 1998-08-12 Acrylic modified waterborne alkyd dispersions
CN98809745A Expired - Fee Related CN1114632C (en) 1997-08-12 1998-08-12 Acrylic modified waterborne sulfonated alkyd dispersions

Family Applications After (1)

Application Number Title Priority Date Filing Date
CN98809745A Expired - Fee Related CN1114632C (en) 1997-08-12 1998-08-12 Acrylic modified waterborne sulfonated alkyd dispersions

Country Status (8)

Country Link
US (2) US6242528B1 (en)
EP (2) EP1003798B1 (en)
JP (2) JP2001512755A (en)
CN (2) CN1174060C (en)
BR (2) BR9811158A (en)
DE (2) DE69824736T2 (en)
ES (2) ES2247713T3 (en)
WO (2) WO1999007759A1 (en)

Families Citing this family (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6333378B1 (en) * 1997-08-12 2001-12-25 Eastman Chemical Company Acrylic modified waterborne alkyd or uralkyd dispersions
CN1174060C (en) * 1997-08-12 2004-11-03 伊斯曼化学公司 Acrylic modified waterborne alkyd dispersions
US6780591B2 (en) 1998-05-01 2004-08-24 Arizona Board Of Regents Method of determining the nucleotide sequence of oligonucleotides and DNA molecules
US7875440B2 (en) 1998-05-01 2011-01-25 Arizona Board Of Regents Method of determining the nucleotide sequence of oligonucleotides and DNA molecules
WO2000073392A2 (en) * 1999-05-27 2000-12-07 Eastman Chemical Company Aqueous alkali resistant printing ink
JP4426144B2 (en) * 1999-06-25 2010-03-03 リゾリューション スペシャルティ マテリアルズ リミティド ライアビリティ カンパニー Quick-drying high solid content coating based on modified alkyd resin
US6818395B1 (en) * 1999-06-28 2004-11-16 California Institute Of Technology Methods and apparatus for analyzing polynucleotide sequences
US6444781B1 (en) * 1999-06-29 2002-09-03 Eastman Chemical Company Polyester resin intermediate compositions and preparation and uses thereof
WO2002010297A2 (en) * 2000-08-02 2002-02-07 Eastman Chemical Company Stable aqueous polymer dispersions and formulations with latex polymers to form waterborne coatings
GB0024504D0 (en) * 2000-10-06 2000-11-22 Avecia Bv Aqueous resin dispersion
EP1207173A1 (en) 2000-11-15 2002-05-22 Eastman Chemical Company Waterborne acrylic modified alkyd
US6699931B2 (en) * 2001-04-09 2004-03-02 Eastman Chemical Company Modified alkyd compositions comprising diol latex compositions and processes of making the same
US20090005476A1 (en) * 2001-04-09 2009-01-01 Eastman Chemical Company Polyol latex compositions and process of making them
US6727314B2 (en) 2001-12-13 2004-04-27 Basf Ag Crosslinking systems for acrylic latex films
CN102408557B (en) * 2001-12-25 2015-01-28 北京万垟防伪技术有限责任公司 Polymer adhesive for water-scraped without set-off intaglio ink composition
US7060745B2 (en) * 2002-04-12 2006-06-13 Resolution Specialty Materials Llc Waterborne acrylate-functionalized alkyd coating compositions
US6780523B2 (en) 2002-04-12 2004-08-24 Eastman Chemical Company Waterborne acetoacetate-functionalized alkyd coating compositions
US6911493B2 (en) 2002-04-12 2005-06-28 Resolution Specialty Materials Llc Acrylate-functionalized alkyd compositions for fast-dry coatings
US6794049B2 (en) * 2002-04-12 2004-09-21 Eastman Chemical Company Fast-dry, high solids coating compositions based on acetoacetate-functionalized alkyd resins
US6946509B2 (en) 2002-09-20 2005-09-20 Resolution Specialty Materials Llc Acrylate-functional alkyd resins having improved dry time
US6683132B1 (en) * 2002-12-19 2004-01-27 Eastman Chemical Company Self-crosslinking aqueous acetoacetate-functionalized sulfonated alkyd systems
CN1329463C (en) * 2003-01-28 2007-08-01 关西油漆株式会社 Aqueous resin composition and aqueous paint composition containing the same
AT412347B (en) * 2003-03-12 2005-01-25 Surface Specialties Austria WATER-DILUTABLE POLYESTER RESINS
US20050004272A1 (en) * 2003-06-23 2005-01-06 Thauming Kuo Small-particle latex compositions based on waterborne alkyd seeds
US7169560B2 (en) 2003-11-12 2007-01-30 Helicos Biosciences Corporation Short cycle methods for sequencing polynucleotides
CA2557177A1 (en) 2004-02-19 2005-09-01 Stephen Quake Methods and kits for analyzing polynucleotide sequences
US7598303B2 (en) * 2005-02-17 2009-10-06 Rohm And Haas Company Process for making an aqueous dispersion
WO2006105306A2 (en) * 2005-03-29 2006-10-05 Arizona Chemical Company Compostions containing fatty acids and/or derivatives thereof and a low temperature stabilizer
US20060270769A1 (en) * 2005-05-24 2006-11-30 Shoaf Glenn L Acrylic-modified alkyd hybrid latexes and their use as viscosity modifiers
US7569157B2 (en) * 2005-06-22 2009-08-04 Hunt Holdings, Inc. Rotted wood stabilizer composition and methods of making and using same
US7666593B2 (en) 2005-08-26 2010-02-23 Helicos Biosciences Corporation Single molecule sequencing of captured nucleic acids
FI120695B (en) * 2006-03-06 2010-01-29 Upm Kymmene Oyj Composites containing acrylic hybrid hybrid resin based on natural fatty acids
JP2007302780A (en) * 2006-05-11 2007-11-22 Kusakabe:Kk Slow-hardenable quick dryable water paint capable of being used together with oil paint
EP2041197B1 (en) * 2006-07-14 2014-11-12 DSM IP Assets B.V. Process for preparing organic nanoparticles
US20080092776A1 (en) * 2006-10-19 2008-04-24 Rebecca Reid Stockl Low-VOC additives for extending wet edge and open times of coatings
US8444758B2 (en) * 2006-10-19 2013-05-21 Eastman Chemical Company Low voc additives for extending the wet edge and open time of aqueous coatings
US20080188588A1 (en) * 2006-12-15 2008-08-07 Sullivan Carl J Waterborne Latex Traffic Paint Compositions Including a Renewable Resource-Based Binder
US9315660B2 (en) * 2007-06-15 2016-04-19 Basf Se Low-VOC aqueous hybrid binders
US20100254917A1 (en) * 2007-07-12 2010-10-07 Matthias Jozef Gertruda Brouns Organic nano-particles and process for their preparation
US7897660B2 (en) * 2007-10-29 2011-03-01 Eastman Chemical Company Incorporation of a resin dispersion to improve the moisture resistance of gypsum products
EP2175000A1 (en) * 2008-10-09 2010-04-14 Cytec Surface Specialties S.A./N.V. Radiation Curable Aqueously Dispersed Alkyd Resin Compositions
EP2342245B1 (en) 2008-10-09 2019-03-06 Allnex Netherlands B.V. Aqueous hybrid dispersions
CN101747500B (en) * 2008-12-12 2012-02-22 上海涂料有限公司技术中心 Sulphonate-base water-reducible alkyd resin and amino baking paint thereof
ATE529488T1 (en) * 2008-12-29 2011-11-15 Rohm & Haas HIGH GLOSS EMULSION PAINTS WITH ADVANCED ALKALYDE
CN101942077B (en) * 2009-07-07 2012-05-30 上海涂料有限公司技术中心 Self-drying water-dilutable alkyd resin containing sulfonate group
US20110086969A1 (en) * 2009-10-09 2011-04-14 Eric Cline Fast dry polyester latex for coatings
US9200177B2 (en) * 2009-10-30 2015-12-01 Dow Global Technologies Llc Alkyd dispersion, and a process for producing the same
EP2365036A1 (en) 2010-03-12 2011-09-14 Cytec Surface Specialties, S.A. Radiation curable aqueous coating compositions
EP2552978B1 (en) 2010-03-31 2020-08-26 Allnex Netherlands B.V. Waterborne hybrid polymer dispersion
US8389591B2 (en) * 2010-08-10 2013-03-05 Valspar Sourcing, Inc. Opaque waterborne UV scratch resistant coatings
CN102712835B (en) * 2010-11-29 2014-10-15 中国医学科学院药用植物研究所 Biomimetic adhesive and preparation method and application thereof
WO2012138348A1 (en) * 2011-04-08 2012-10-11 Dow Global Technologies Llc A coating compositon, and a process for producing the same
RU2492332C1 (en) * 2012-06-04 2013-09-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Национальный исследовательский университет "МЭИ" Method to intensify condensation of steam in condenser of steam-turbine plant
CN102827501A (en) * 2012-08-02 2012-12-19 中山大桥化工企业集团中山智亨实业发展有限公司 Double-curing varnish paint
EP2945994B1 (en) 2013-01-18 2018-07-11 Basf Se Acrylic dispersion-based coating compositions
CN104072740A (en) * 2014-06-20 2014-10-01 安徽华箔箔业科技有限公司 Aqueous-dispersion alkyd resin synthesis process
ES2883860T3 (en) 2014-11-03 2021-12-09 Arkema Inc Latex comprising water soluble acrylic modified alkyd dispersion and method of producing it
TWI713498B (en) 2015-03-24 2020-12-21 美商羅門哈斯公司 Core-shell aqueous latex
RU2602653C1 (en) * 2015-05-06 2016-11-20 федеральное государственное бюджетное образовательное учреждение высшего образования "Национальный исследовательский университет "МЭИ" (ФГБОУ ВО "НИУ "МЭИ") Method of intensifying heat exchange in condenser of steam turbine plant
CN104927605A (en) * 2015-05-30 2015-09-23 广东华兹卜化学工业有限公司 Water-based alkyd carpentry paint and preparation method thereof
SG11202109832PA (en) * 2019-03-19 2021-10-28 Harima Chemicals Inc Resin composition for aqueous coating materials, and coating film
US20220363962A1 (en) * 2021-05-13 2022-11-17 Ingevity South Carolina, Llc Uv or eb curable multifunctional tall oil (meth)acrylates
CN114395085B (en) * 2022-01-24 2024-01-16 浙江天女集团制漆有限公司 Water-based modified polyester resin and preparation method and application thereof

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3345313A (en) 1963-02-20 1967-10-03 Trojan Powder Co Alkyd resins and their preparation from reaction mixtures comprising a polymethylolalkanoic acid
US3734874A (en) 1970-02-27 1973-05-22 Eastman Kodak Co Polyesters and polyesteramides containing ether groups and sulfonate groups in the form of a metallic salt
US3778395A (en) 1972-02-18 1973-12-11 Borden Inc Printing inks comprising a uralkyd
IT981904B (en) 1973-04-09 1974-10-10 Duco Spa WATER-BASED ALCOHID RESINS MODI FICATED WITH ACRYLIC OR META CRYLIC ACID
US3979346A (en) 1973-11-08 1976-09-07 Vianova-Kunstharz A.G. Emulsifiers for preparing aqueous dispersions of alkyd resins
US4011388A (en) 1974-07-02 1977-03-08 E. I. Du Pont De Nemours And Company Process for preparing emulsions by polymerization of aqueous monomer-polymer dispersions
DE2440267C2 (en) 1974-08-22 1984-10-11 Bayer Ag, 5090 Leverkusen Thixotropic urethane alkyd resins
US4178425A (en) 1976-07-07 1979-12-11 Rohm And Haas Company Polyurethane coating compositions containing unsaturated esters of glycol monodicyclopentenyl ethers
EP0000087B1 (en) 1977-06-13 1981-09-09 Unilever N.V. Aqueous air-drying alkyd dispersions and their use
US4116902A (en) 1977-10-05 1978-09-26 International Minerals & Chemical Corp. Polyurethane-modified alkyd resin
US4180645A (en) 1978-05-22 1979-12-25 Rohm And Haas Company Polyurethane coating compositions from dicyclopentenyl acrylate and/or methacrylate
US4222911A (en) 1978-08-07 1980-09-16 Ppg Industries, Inc. Polyester diol extended uralkyd resin and coating compositions containing the same
US4293471A (en) 1979-03-16 1981-10-06 E. I. Du Pont De Nemours And Company Fast-drying alkyd latex
JPS5641221A (en) 1979-09-10 1981-04-17 Hitachi Chem Co Ltd Water-dispersed resin composition
AT365216B (en) 1979-10-29 1981-12-28 Vianova Kunstharz Ag METHOD FOR PRODUCING WATER-EMULSIBLE AIR-DRYING VARNISH BINDERS BASED ON MODIFIED ALKYD RESIN AND EMULSIONS BASED ON THIS BASE
US4414357A (en) 1979-11-27 1983-11-08 Glasurit America, Inc. Polyester or alkyd resin composition containing acrylic microgels
EP0094386B1 (en) * 1981-06-29 1986-03-05 Dulux Australia Ltd Stable aqueous film-forming dispersions
DE3132937A1 (en) * 1981-08-20 1983-03-03 Henkel KGaA, 4000 Düsseldorf WATER-DISCOVERABLE RESIN PREPARATION BASED ON ALKYD RESIN AND POLYACRYLATE RESIN AND THEIR USE AS WATER-DISCOVERABLE PATENT RESIN
US4436849A (en) * 1981-10-26 1984-03-13 Kansai Paint Company, Limited Aqueous resin composition
CA1208835A (en) * 1982-10-04 1986-07-29 Teruaki Kuwajima Aqueous coating composition
DE3246614A1 (en) 1982-12-16 1984-06-20 Henkel KGaA, 4000 Düsseldorf EMULSATOR AND SOLVENT-FREE ALKYD RESIN WATER PAINT
US4737551A (en) 1986-06-23 1988-04-12 E. I. Dupont De Nemours And Company Coating composition of a hydroxy group-containing modified polyester with polymerized lactone monomers
US4698391A (en) 1986-07-30 1987-10-06 Eastman Kodak Company Crosslinked polymers with lowered resistivity and materials and methods for their preparation
US4916181A (en) * 1987-09-29 1990-04-10 Ppg Industries, Inc. Water-borne acrylic/polyester resin
JPH02214787A (en) 1989-02-14 1990-08-27 Nippon Paint Co Ltd Cold drying coating composition
JPH0672175B2 (en) * 1989-08-22 1994-09-14 昭和高分子株式会社 Photocurable composition
US5011883A (en) 1990-02-07 1991-04-30 Ici Americas Inc. Stabilized polymer latex composition
IT1241142B (en) 1990-05-16 1993-12-29 Alusuisse Italia Spa ACCELERATING MONOMERS OF THE POLYMERIZATION OF UNSATURE POLYESTER RESINS
FR2664533B1 (en) 1990-07-16 1994-09-30 Rhone Poulenc Films COMPOSITE POLYESTER FILMS AND THEIR USE AS PROTECTIVE LAYER FOR PHOTOPOLYMER PLATES AND PHOTOPOLYMER PLATES COMPRISING THE SAME.
DE69124354T3 (en) 1990-12-21 2003-04-24 Rohm And Haas Co., Philadelphia Air-curing polymer composition
EP0555903A1 (en) 1992-02-04 1993-08-18 Akzo Nobel N.V. Water-dispersible hybrid core-shell polymer, an aqueous dispersion thereof, and a coating composition made therefrom
US5296530A (en) 1992-07-28 1994-03-22 Rohm And Haas Company Method for light-assisted curing of coatings
US5349026A (en) 1992-11-20 1994-09-20 Rohm And Haas Company Reactive coalescents
US5326808A (en) 1993-02-18 1994-07-05 The Glidden Company Odor free, air dry, aqueous emulsion paints
US5371148A (en) 1993-06-23 1994-12-06 Union Carbide Chemicals & Plastics Technology Corporation Reactive polymers having pendant flexible side chains prepared from ethylenically unsaturated carbodiimides
BE1007263A3 (en) 1993-07-09 1995-05-02 Dsm Nv Alkyd resin and emulsions thereof.
US5525662A (en) 1993-07-14 1996-06-11 Rohm And Haas Company Functionalization of polymers via enamine of acetoacetate
US5686518A (en) 1993-10-12 1997-11-11 Georgia Tech Miniemulsion polymerization process using polymeric co-surfactant
US5378757A (en) 1993-11-15 1995-01-03 Eastman Chemical Company Water-dissipatable alkyd resins and coatings prepared therefrom
AT400719B (en) * 1994-04-07 1996-03-25 Vianova Kunstharz Ag METHOD FOR PRODUCING WATER-THINNABLE AIR-DRYING LACQUER AND THE USE THEREOF
US5539073A (en) 1995-04-12 1996-07-23 Eastman Chemical Company Waterborne polymers having pendant allyl groups
US5538760A (en) 1995-05-22 1996-07-23 Eastman Chemical Company Alkyd/acrylic latexes for cleaning and protecting hard surfaces
US5569715A (en) 1995-07-24 1996-10-29 Basf Corporation Process for obtaining hydrophobically modified emulsion polymers and polymers obtained thereby
CN1174060C (en) * 1997-08-12 2004-11-03 伊斯曼化学公司 Acrylic modified waterborne alkyd dispersions

Also Published As

Publication number Publication date
US6242528B1 (en) 2001-06-05
EP1003798B1 (en) 2005-10-19
ES2218848T3 (en) 2004-11-16
WO1999007759A1 (en) 1999-02-18
BR9811167A (en) 2000-07-25
DE69824736D1 (en) 2004-07-29
DE69824736T2 (en) 2004-10-21
BR9811158A (en) 2000-07-25
WO1999007799A1 (en) 1999-02-18
US6262149B1 (en) 2001-07-17
JP2001512755A (en) 2001-08-28
JP2001512778A (en) 2001-08-28
CN1272854A (en) 2000-11-08
ES2247713T3 (en) 2006-03-01
CN1114632C (en) 2003-07-16
EP1003820B1 (en) 2004-06-23
DE69831955T2 (en) 2006-04-27
EP1003820A1 (en) 2000-05-31
DE69831955D1 (en) 2006-03-02
CN1272865A (en) 2000-11-08
EP1003798A1 (en) 2000-05-31

Similar Documents

Publication Publication Date Title
CN1174060C (en) Acrylic modified waterborne alkyd dispersions
CN1131252C (en) Acrylic modified waterborne alkyd or uralkyd dispersions
US6844390B2 (en) Modified alkyd compositions comprising polyol latex compositions and processes of making them
CN1659209A (en) Waterborne acetoacetate-functionalized alkyd coating
EP1726604B1 (en) Acrylic modified alkyl hybrid latexes, coating composition, method of increasing and adjusting the viscosity and substrate coated
CN106478899A (en) A kind of modification light curing resin composition and preparation method thereof
CN1646646A (en) Acrylate-functionalized alkyd compositions for fast-dry coatings
US6699931B2 (en) Modified alkyd compositions comprising diol latex compositions and processes of making the same
EP3215546B1 (en) Latex comprising water-soluble acrylic modified alkyd dispersion and method of production thereof
US20050004272A1 (en) Small-particle latex compositions based on waterborne alkyd seeds
MXPA00001407A (en) Acrylic modified waterborne alkyd dispersions
US20090005476A1 (en) Polyol latex compositions and process of making them
CN117597391A (en) Crosslinkable acrylic modified epoxy coating compositions
JPH01129072A (en) Resin composition for water paint
MXPA00001337A (en) Acrylic modified waterborne sulfonated alkyd dispersions

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C56 Change in the name or address of the patentee

Owner name: EASTMAN CHEMICAL COMPANY

Free format text: FORMER NAME OR ADDRESS: YISIMAN CHEMICAL COMPANY

CP01 Change in the name or title of a patent holder

Address after: Tennessee

Patentee after: EASTMAN CHEMICAL Co.

Address before: Tennessee

Patentee before: EASTMAN CHEMICAL Co.

ASS Succession or assignment of patent right

Owner name: HEKE XI'AN SPECIAL CHEMICAL PRODUCT CO.,LTD.

Free format text: FORMER OWNER: EASTMAN CHEMICAL COMPANY

Effective date: 20090918

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20090918

Address after: Ohio, USA

Patentee after: Hurco Xi'an special chemicals Co.

Address before: Tennessee

Patentee before: EASTMAN CHEMICAL Co.

C56 Change in the name or address of the patentee
CP01 Change in the name or title of a patent holder

Address after: Ohio, USA

Patentee after: MOMENTIVE SPECIALTY CHEMICALS Inc.

Address before: Ohio, USA

Patentee before: Momentive Specialty Chemicals GmbH

Address after: Ohio, USA

Patentee after: MOMENTIVE SPECIALTY CHEMICALS GmbH

Address before: Ohio, USA

Patentee before: Hurco Xi'an special chemicals Co.

CX01 Expiry of patent term

Granted publication date: 20041103

CX01 Expiry of patent term